Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14. - Wikidata - awgldk - TriplyDB

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

http://www.wikidata.org/entity/Q34483729

about

Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene family Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).A locus for febrile seizures (FEB3) maps to chromosome 2q23-24 Ion channels and epilepsy Cognitive effects of nicotine: genetic moderators.An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder Partial epilepsy with pericentral spikes: a new familial epilepsy syndrome with evidence for linkage to chromosome 4p15.RBFOX1 and RBFOX3 mutations in rolandic epilepsy Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes.Recent advances in the genetics of epilepsy: insights from human and animal studies.Genetics of childhood epilepsy Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.Atypical evolutions of benign localization-related epilepsies in children: are they predictable?Properties underlying the influence of nicotinic receptors on neuronal excitability and epilepsy.Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.Identification of epilepsy genes in human and mouse 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.Progress in the genetics of the partial epilepsies.The copy number variant involving part of the alpha7 nicotinic receptor gene contains a polymorphic inversion.Benign childhood focal epilepsies: assessment of established and newly recognized syndromes.Genetics in epilepsy: transcultural perspectives.Genetics of inherited human epilepsies Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.Genetic focal epilepsies: state of the art and paths to the future.Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gating A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.Neuropsychological deficits in childhood epilepsy syndromes.A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy.Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome.Genetics of the epilepsies: where are we and where are we going?Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy.Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.Clinical features of benign epilepsy of childhood with centrotemporal spikes in chinese children Genotype to phenotype-discovery and characterization of novel genomic disorders in a "genotype-first" era.Delineation of 15q13.3 microdeletions.New genes for focal epilepsies with speech and language disorders.Childhood absence epilepsy and benign epilepsy with centro-temporal spikes: a narrative review analysis.A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2.

P2860

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P2860

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

http://www.wikidata.org/entity/Q34483729

description

1998 nî lūn-bûn

@nan

1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

name

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@ast

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@en

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@nl

type

label

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@ast

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@en

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@nl

prefLabel

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@ast

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@en

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

@nl

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Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

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Bretscher C

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Eeg-Olofsson O

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Fiedler B

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Himmelein B

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Kurlemann G

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Kämpfer F

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Lässker U

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Moldenhauer K

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Neubauer BA

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Schwabe G

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1608-1612

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scholarly article

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10.1212/WNL.51.6.1608

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6

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9855510

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